Informatie:
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ID
31853
Beschrijving
A Study of Immune Cells in Patients With Rheumatoid Arthritis During Different Types of Anti-TNF Alpha Treatments (Study P05521); ODM derived from: https://clinicaltrials.gov/show/NCT00724672
Link
https://clinicaltrials.gov/show/NCT00724672
Trefwoorden
Versies (1)
- 04-10-18 04-10-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
4 oktober 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Rheumatoid Arthritis NCT00724672
Eligibility Rheumatoid Arthritis NCT00724672
- StudyEvent: Eligibility
Similar models
Eligibility Rheumatoid Arthritis NCT00724672
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Rheumatoid Arthritis Disease activity score das28
Item
must have active ra (das28 >5.1)
boolean
C0003873 (UMLS CUI [1,1])
C4481729 (UMLS CUI [1,2])
C4481729 (UMLS CUI [1,2])
Bone erosion X-ray
Item
must have x-ray evidence of an erosive disease,
boolean
C0587240 (UMLS CUI [1,1])
C0034571 (UMLS CUI [1,2])
C0034571 (UMLS CUI [1,2])
Patient Eligible Anti-TNF therapy | Anti-TNF therapy Absent
Item
must be eligible for but have never received any anti-tnf treatment,
boolean
C0030705 (UMLS CUI [1,1])
C1548635 (UMLS CUI [1,2])
C0281481 (UMLS CUI [1,3])
C0281481 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C1548635 (UMLS CUI [1,2])
C0281481 (UMLS CUI [1,3])
C0281481 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
ACR Criteria Fulfill Rheumatoid Arthritis
Item
must fulfill the 1987 criteria of the american college of rheumatology classification criteria for a diagnosis of ra, for at least 3 months,
boolean
C3273747 (UMLS CUI [1,1])
C1550543 (UMLS CUI [1,2])
C0003873 (UMLS CUI [1,3])
C1550543 (UMLS CUI [1,2])
C0003873 (UMLS CUI [1,3])
Standard therapy failed | Methotrexate | leflunomide
Item
must have failed standard therapy (methotrexate or leflunomide).
boolean
C2936643 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
C0025677 (UMLS CUI [2])
C0063041 (UMLS CUI [3])
C0231175 (UMLS CUI [1,2])
C0025677 (UMLS CUI [2])
C0063041 (UMLS CUI [3])
Pregnancy | Breast Feeding
Item
must not be a women who is pregnant or breastfeeding,
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Malignant Neoplasms
Item
must not have a history of any malignancy,
boolean
C0006826 (UMLS CUI [1])
Communicable Disease
Item
must not have an active infection,
boolean
C0009450 (UMLS CUI [1])
Susceptibility Communicable Disease
Item
must not be prone to infection,
boolean
C0220898 (UMLS CUI [1,1])
C0009450 (UMLS CUI [1,2])
C0009450 (UMLS CUI [1,2])
Tuberculosis | Hepatitis B | Hepatitis C | HIV Infection
Item
must not have tuberculosis, hepatitis b, hepatitis c, or hiv,
boolean
C0041296 (UMLS CUI [1])
C0019163 (UMLS CUI [2])
C0019196 (UMLS CUI [3])
C0019693 (UMLS CUI [4])
C0019163 (UMLS CUI [2])
C0019196 (UMLS CUI [3])
C0019693 (UMLS CUI [4])
Arthritis, Infectious | Joint Prosthesis Native
Item
must not have septic arthritis of a native prosthetic joint within the last 12 months,
boolean
C0003869 (UMLS CUI [1])
C0022417 (UMLS CUI [2,1])
C0175649 (UMLS CUI [2,2])
C0302891 (UMLS CUI [2,3])
C0022417 (UMLS CUI [2,1])
C0175649 (UMLS CUI [2,2])
C0302891 (UMLS CUI [2,3])
Heart failure New York Heart Association Classification
Item
must not have nyha grade 3 or 4 heart failure,
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,2])
Demyelinating Disease | Lupus Erythematosus, Systemic
Item
must not have a history of demyelinating disease or systemic lupus erythematosis.
boolean
C0011303 (UMLS CUI [1])
C0024141 (UMLS CUI [2])
C0024141 (UMLS CUI [2])